HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304409Generated: October 31, 2026
Sodium Hydroxide → (+)-5-[[(2R,4S)-4-hydroxy-1-(4-methoxyphenethyl)pyrrolidin-2-yl]methyl]-5,11-dihydrodibenzo[b,e][1,4]oxazepine
https://huagongshe.com/reaction/2304409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (+)-5-[[(2R, 4S)-4-benzoyloxy-1-(4-methoxyphenethyl)pyrrolidin-2-yl]methyl]-5,11-dihydrodibenzo[b,e][1,4]oxazepine | HCID 15481941 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (+)-5-[[(2R,4S)-4-hydroxy-1-(4-methoxyphenethyl)pyrrolidin-2-yl]methyl]-5,11-dihydrodibenzo[b,e][1,4]oxazepine | HCID 15481940 | 97.1% |
Reaction Steps
To 870 mg (1.63 mmol) of (+)-5-[[(2R, 4S)-4-benzoyloxy-1-(4-methoxy phenethyl)pyrrolidin-2-yl]methyl]-5,11-dihydrodibenzo[b,e][1, 4]oxazepine in 15 ml of ether was added 460 mg (11.4 mmol) of NaOH in methanol (60 ml) and the mixture was stirred at room temperature for 1 hour. The mixture was concentrated in vacuo, then water was added to the residue and the products were extracted with ether. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified by silicagel column chromatography (ethyl acetate) to give 680 mg (97.1%) of (+)-5-[[(2R, 4S)-4-hydroxy-1-(4-methoxyphenethyl) pyrrolidin-2-yl]methyl]-5,11-dihydrodibenzo[b,e][1,4]oxazepine as yellow amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06436922B1 |
|---|
| Source dataset | uspto-grants-2002_08 |
|---|
| ORD ID | ord-2d757a6b04704100bca0c44a0ab7a700 |
|---|
| Source note | uspto-grants-2002_08 |
|---|